KO Validated Antibodies 2
Anti-PHGDH Antibody (CAB19974)[KO Validated]
- SKU:
- CAB19974
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Metabolism
Description
Antibody Name: | Anti-PHGDH Antibody [KO Validated] |
Antibody SKU: | CAB19974 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant protein of human PHGDH. |
Application: | WB IF |
Recommended Dilution: | WB 1:500 - 1:2000 IF 1:50 - 1:200 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | HeLa |
Immunogen: | Recombinant protein of human PHGDH. |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | Email for sequence |
Gene ID: | 26227 |
Uniprot: | O43175 |
Cellular Location: | |
Calculated MW: | 56kDa |
Observed MW: | 57KDa |
Synonyms: | PHGDH, 3-PGDH, 3PGDH, HEL-S-113, NLS, NLS1, PDG, PGAD, PGD, PGDH, PHGDHD, SERA |
Background: | This gene encodes the enzyme which is involved in the early steps of L-serine synthesis in animal cells. L-serine is required for D-serine and other amino acid synthesis. The enzyme requires NAD/NADH as a cofactor and forms homotetramers for activity. Mutations in this gene have been found in a family with congenital microcephaly, psychomotor retardation and other symptoms. Multiple alternatively spliced transcript variants have been found, however the full-length nature of most are not known. |
UniProt Protein Function: | PHGDH: Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency (PHGDH deficiency). It is characterized by congenital microcephaly, psychomotor retardation, and seizures. Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. |
UniProt Protein Details: | Protein type:Oxidoreductase; Amino Acid Metabolism - glycine, serine and threonine; EC 1.1.1.95; Cell development/differentiation Chromosomal Location of Human Ortholog: 1p12 Cellular Component: cytosol Molecular Function:electron carrier activity; NAD binding; phosphoglycerate dehydrogenase activity Biological Process: neural tube development; glial cell development; glycine metabolic process; gamma-aminobutyric acid metabolic process; glutamine metabolic process; L-serine biosynthetic process; spinal cord development; regulation of gene expression; amino acid biosynthetic process; brain development; taurine metabolic process; neurite development; threonine metabolic process Disease: Phosphoglycerate Dehydrogenase Deficiency; Neu-laxova Syndrome 1 |
NCBI Summary: | This gene encodes the enzyme which is involved in the early steps of L-serine synthesis in animal cells. L-serine is required for D-serine and other amino acid synthesis. The enzyme requires NAD/NADH as a cofactor and forms homotetramers for activity. Mutations in this gene have been found in a family with congenital microcephaly, psychomotor retardation and other symptoms. Multiple alternatively spliced transcript variants have been found, however the full-length nature of most are not known. [provided by RefSeq, Aug 2011] |
UniProt Code: | O43175 |
NCBI GenInfo Identifier: | 21264510 |
NCBI Gene ID: | 26227 |
NCBI Accession: | O43175.4 |
UniProt Secondary Accession: | O43175,Q5SZU3, Q9BQ01, B2RD08, |
UniProt Related Accession: | O43175 |
Molecular Weight: | 533 |
NCBI Full Name: | D-3-phosphoglycerate dehydrogenase |
NCBI Synonym Full Names: | phosphoglycerate dehydrogenase |
NCBI Official Symbol: | PHGDH |
NCBI Official Synonym Symbols: | NLS; PDG; PGD; NLS1; PGAD; PGDH; SERA; 3PGDH; 3-PGDH; PHGDHD; HEL-S-113 |
NCBI Protein Information: | D-3-phosphoglycerate dehydrogenase; epididymis secretory protein Li 113 |
UniProt Protein Name: | D-3-phosphoglycerate dehydrogenase |
UniProt Gene Name: | PHGDH |
UniProt Entry Name: | SERA_HUMAN |